US5330631A - Aluminium smelting cell - Google Patents

Aluminium smelting cell Download PDF

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Publication number
US5330631A
US5330631A US07/969,850 US96985093A US5330631A US 5330631 A US5330631 A US 5330631A US 96985093 A US96985093 A US 96985093A US 5330631 A US5330631 A US 5330631A
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Prior art keywords
anode
cell
shaped structures
cathode
metal
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US07/969,850
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Draco D. Juric
Raymond W. Shaw
Geoffrey J. Houston
Ian A. Coad
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Rio Tinto Aluminium Ltd
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Comalco Aluminum Ltd
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Assigned to COMALCO ALUMINUM LIMITED reassignment COMALCO ALUMINUM LIMITED ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: COAD, IAN A., HOUSTON, GEOFFREY J., JURIC, DRAGO D., SHAW, RAYMOND W.
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    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25C—PROCESSES FOR THE ELECTROLYTIC PRODUCTION, RECOVERY OR REFINING OF METALS; APPARATUS THEREFOR
    • C25C3/00—Electrolytic production, recovery or refining of metals by electrolysis of melts
    • C25C3/06—Electrolytic production, recovery or refining of metals by electrolysis of melts of aluminium
    • C25C3/08—Cell construction, e.g. bottoms, walls, cathodes

Definitions

  • This invention relates to improvements in aluminium smelting cells.
  • the patent literature also discloses the use of wettable materials (TIB 2 based) which protrude from the metal pad as platforms or pedestals to yield an active cathode surface. These give a power reduction through reduced ACD but the effect is limited due to no gain in bubble release mechanisms at the anode. These types of cells have not been proven commercially viable, presumably because of a combination of material problems and the cost of construction. The cathode area available beneath the anode is also reduced compared to that of a flat metal pad when platforms or pedestals are used. In this type of cell the metal pad plays little role in carrying active current in the cell operations and is regarded as "non-active".
  • Stedman et al (Australian Patent Application No. 50008/90 and U.S. Ser. No. 07/481847) have developed cells with improved performance by the use of a shaped cathode to induce shaping in the anodes to yield a anode having a double slope arrangement including a continuous longitudinal slope of the type envisaged by Boxall et al in U.S. Pat. No. 4,602,990, or having an induced bevelled section at its longitudinal edges.
  • the invention provides an aluminium smelting cell comprising side walls and a floor defining a cathode surface, at least one anode having an active electrode surface spaced from and substantially parallel to said cathode surface to define an interelectrode gap, characterized by said cathode surface being substantially horizontal in the longitudinal direction of said anode(s) and by shaped structures projecting from said cathode surface, said structures being covered by wetted cathode material and being shaped to modify the current distribution between the anode(s) and the cathode whereby current flows through said shaped structures and through the remaining cathode portions to cause preferential shaping of the anode(s) to encourage shortening of the release path of bubbles under said anode(s) to thereby minimize cell resistivity and enable operation at a reduced anode to cathode distance.
  • horizontal means a slope of no greater than about 2° in the longitudinal direction of the anodes.
  • cathode regions adjacent the shaped cathode structures remain active as cathode areas and do not substantially increase cathode current density over that found in conventional cells.
  • Other cells having cathode protrusions (or pedestals) are active essentially only on the protruding areas thereby resulting in increased cathodic current density.
  • the metal level in the substantially flat cathode regions may vary from the fully drained mode up to a depth of 10 cm or more depending on the height of the shaped structures. To gain the full benefit from the new cell design, the depth should not exceed that of the shaped structures for an extended time period as this will prevent the anodes profiling to provide the desired bubble releases. This enables metal storage throughout the entire cell and removes the need for a large and invasive sump and/or for short tapping cycles. Advantages of simpler cell construction, elimination of a substantial sump as a weak point in cell construction and better plant operations result from the use of such shaped structures.
  • the metal level may be allowed to rise above the level of the shaped structures for limited time periods after anode profiling has occurred, and in certain circumstances this can be additionally advantageous, e.g. as a temporary increase in metal reserve storage. With this design the cells are able to revert to the intended mode of operation with a metal pad, if such an operation is desired.
  • the new cell design therefore allows flexibility of cell operation as either:
  • These shaped structures can be built as an integral part of a new cell or can be retrofitted to cells, possibly as modular inserts or sections in an existing cell, which may or may not have a wetted horizontal cathode surface, without necessarily being bonded or fixed to the cathode surface.
  • the metal provides the necessary conductive path and the modular inserts will have sufficient density and mass to remain in position without fixing or bonding. This provides a distinct advantage since bonding and fixing of wettable surfaces to the base of the cell is a widely recognized problem in the construction of aluminium smelting cells containing wettable cathodes.
  • the shaping of anodes to provide enhanced bubble release is important for reducing the resistance in the ACD. Additionally the shaping of anodes to obtain the semi-continuous and gradual release of bubbles by strategically-placed cathode protrusions was also found to be especially important for the stable operation of the present cells when a metal pad of significant thickness (i.e. under non-thin film conditions) resides as an active cathode.
  • FIG. 1 is a schematic end elevation of a typical anode cathode protrusion combination embodying the invention
  • FIG. 1A is an end elevation schematically illustrating a modification to the embodiment of FIG. 1;
  • FIG. 2 is a end elevation similar to FIG. 1 showing a schematic representation of an anode and triangular cathode protrusion combination according to a second embodiment of the invention
  • FIGS. 3 and 4 show further embodiments of the invention in which the cathode protrusions are rectangular and are arranged at various spacings;
  • FIG. 5 is a partly schematic perspective view of a cathode and anode arrangement based on the principal shown in FIG. 4 of the drawings;
  • FIG. 6 is a schematic representation of the anode shaping produced by the embodiment of FIG. 5;
  • FIG. 7 is a partly schematic perspective view of a cathode and anode arrangement based on the principle shown in FIG. 2 of the drawings;
  • FIG. 8 is an end elevation representation of the anode and cathode profiles measured in a test cell constructed according to the embodiment of FIG. 7;
  • FIGS. 9A and 9B are schematic representations of the 5% current distribution lines produced for the embodiments of FIGS. 5 and 7;
  • FIG. 10 is a graph showing the relationship between electrolyte resistivity ratio and anode to cathode distance for three different cell constructions
  • FIG. 11 is a graph showing resistivity ratio against anode angle 435 mm bubble path length, 1.1 A/cm 2 anode current density
  • FIG. 12 is a graph of resistivity ratio against bubble path length (4 degree anode, 1.1 A /cm 2 anode current density);
  • FIG. 13 is a schematic plan view of a cathode protrusion arrangement according to another embodiment of the invention.
  • FIG. 14 is a sectional side elevation taken along the line 14--14 in FIG. 13.
  • each anode 1 has two associated spaced projections 2,3 of generally rounded triangular cross-section formed in the surface of the cathode 4, having an embedded current collector bar C, adjacent either side of each anode 1.
  • the projections 2,3 may be formed as part of the construction of the cathode 4 of the cell or may be retro-fitted to an existing cell in any suitable manner known in the art.
  • eachprojection 2,3 and the intervening cathode surface 4 is covered by a suitable wetted cathode material, such as a TiB 2 -containing composite of the type known in the art.
  • a suitable wetted cathode material such as a TiB 2 -containing composite of the type known in the art.
  • the positioning of the projectionsas shown in FIG. 1 will cause the longitudinal edges 5,6 of the anode 1 to be burnt away or profiled to the shape shown to thereby encourage bubble release and adequate bath circulation.
  • a pool of metal 7 collects between the projections 2,3, and this pool may be controlled to be of any desired depth including above the top of the projections 2 and 3, although this depth of metal should not be maintained for a prolonged period (more than a few days) otherwise the anode profiling will be lost and the anode will revert to a standard flat bottomed anode.
  • the dimensions employed (X, Y, Z) and the depth of the metal pool 7 can vary over a considerable range depending upon the total cell dimensions, the anode dimensions and the operating system desired.
  • the separation of the protrusions (X) is largely set by the anode size with the desired system having protrusions towards each edge of the anode.
  • Typical anodes currently used in cells can range from under 400 mm to over 800 mm wide.
  • the height and shape of the protrusions depends upon the depth of metal desired (for storage) and upon the desired shape of and degree of profiling or rounding of the anodes.
  • anode such as used in theapplicant's trials referred to below, this would typically be of the order of 50-100 mm (dimension Z) but this can readily be changed.
  • the size of the protrusion as set by dimensions Y and Z depends upon the degree of profiling or rounding desired to be induced in the anode. Typically dimension Y would be of the order of 2-5 times dimension Z but the range can extend beyond that in special cases.
  • the depth of metal used can vary as in trials of the cell shown in FIGS. 5 from ⁇ 5 mm up to the height of the protrusions (>100 mm) depending on needs.
  • additional protrusions may be added within this area as baffles to reduce any metal movement and to maintain a defined ACD that induces the profiling on tapping the metal out.
  • FIG. 1A of the drawings One suitable modification of this typeis shown in FIG. 1A of the drawings in which additional smaller projections2A, 2B, 3A, 3B are formed between the main projections 2 and 3.
  • the projections become progressively smaller and may be necessary to maintain a defined ACD that induces the profiling when the depth of the metal pool is reduced below the level of the additional protrusions.
  • the additional protrusions may take any desired form and may even be constituted by an array of upstanding cubic structures suitably positioned to provide the necessary defined ACD and to reduce unwanted metal movement in a large cell having wide anodes.
  • two generally triangular projections or protrusions 8,9 are formed on the surface of thecathode 10 immediately under each anode 11 such that a generally V-shaped profile is present under each anode.
  • This causes the edges 12,13 of the anode 11 to be burnt away in the manner shown in FIG. 2 to thereby encourage efficient bubble release and bath circulation.
  • the surfaces defining the V-profile are inclined at about 4° to the horizontal.
  • a pool of metal 14 of variable depth is held between the projections 8 and 9.
  • generally rectangular projections 15,16 are formed in the surface of the cathode 17 and cause shaping of the edges 18,19 of the anode 20 in the manner shown in the figure.
  • the dimensions x and y may vary quite considerably as shownin FIG. 4, although in each embodiment a central generally rectangular channel of varying dimensions is defined within which a pad of metal 21 ofvarying depth collects under each anode 20.
  • the shaping of the edges 18,19 proceeds further inwardly of the anode 20 to define a downwardly extending peak 22 as shown.
  • the projections or protrusions 8 and 9, and 15 and 16 extend along the longitudinal edges ofthe anode and may terminate centrally of the cell in a flat cathode surfaceor in a less pronounced depressed central metal collection channel or trench.
  • a side channel may be provided or the projections may abut directly against the side wall.
  • transverse protrusions of the type shown in FIGS. 13 and 14 described further below, or in FIG. 15 of Australian Paten Application No. 50008/90 may be provided to provide bevelling of the side edges and/or end edges ofthe anodes for the reasons discussed in our earlier patent application above.
  • a cell constructed in accordance with the embodiment of FIG. 2 of the drawings would be similar in construction to the embodiment of FIG. 10of the drawings which will be described in greater detail below.
  • FIG. 5 of the drawings A further embodiment developed from the principle shown in FIG. 4 of the drawings is shown in greater detail in FIG. 5 of the drawings, in which the side walls and end walls of the cell have been omitted for greater clarity.
  • the cathode 24 is formed with two rectangulararrays of pairs of rectangular projections 25,26 and 27,28 positioned on either side of a central metal collection channel 29 and separated by longitudinal and transverse slots 30,31 and 32,33, within which pools of metal may be allowed to collect, in the manner shown in FIG. 4, for eventual discharge into the central channel 29.
  • a suitable wetted cathode material such as a TiB 2 -containing composite of the type known in the art.
  • An array of anodes 34 is positioned in overlying relationship with the array of protrusions 25,26 and 27,28, although the anodes over the array of protrusions 27,28 has been excluded for clarity and the array of anodes over the array of protrusions 25,26 is shown at an exaggerated elevated position also for reasons of clarity.
  • the shadow 35 of one anode is illustrated in FIG. 5.
  • the cell design shown schematically in FIG. 5 of the drawings was trialled in a 90,000 A reduction cell having twenty anodes each 865 mm long by 525 mm wide.
  • the cell was operated with three different slot widths to determine the height H of the peak 36 associated with each slot 31,33 located centrally of each anode 34.
  • the slot was 80 mm deep in a TiB 2 composite approximately 100 mm deep over a cathode block approximately 220 mm deep.
  • Table 1 The results obtained are detailed in Table 1 below.
  • the peak 36 is shown schematically in FIG. 6 of the drawings.
  • FIG. 9A of the drawings represents part of a half end section of one anode and corresponding cathode according to FIG. 5 showing the 5% current distribution lines applicable to the anode and cathode structures shown.
  • the current distribution lines indicate that current is conducted through both the protrusions 25,26 and through the cathode areas 24 within the slots 30 and 31 via the metal M stored in the slots 30 and 31.
  • the profileinduced in the active face of the anode as a result of the current distribution shown is clearly evident, and it will be appreciated that a similar, although more elongate, profile will be induced in the longitudinal direction of the anode.
  • FIG. 2 of the drawings was similarly trialled in a 100,000 A reduction cell having anodes 865 mm ⁇ 525 mm.
  • This test cell is shown schematically in FIG. 7 of the drawings in which an array of triangular protrusions 8 and 9 is positioned on either side of a central metal collection channel 36, with each array of protrusions 8 and 9 havingoverlying anodes 13 (with one array excluded for clarity).
  • the profile formed on the active face of each anode 13 as the cell operates corresponds to the profile of the cathode 10 between the respective protrusions 8 and 9 and is a more accurate representation of the actual profile which is burnt into the active face of the anode 13 than the schematic profile shown in FIG. 2 of the drawings.
  • FIG. 8 of the drawings is a representation of the actual anode profile achieved in the cell shownin FIG. 7 of the drawings by the use of the cathode protrusions shown.
  • FIG. 9B shows the 5% current distribution diagram for the cell of FIG. 7 showing the effect of current distribution in shaping the anode 13 in the manner shown.
  • the object of the trial using the cell of FIG. 7 of the drawings was to achieve a reduced cell voltage at an anode to cathode distance (ACD) of 20mm whilst employing a conventional electrolyte chemistry (approx. 10% excess aluminium fluoride, 4% calcium fluoride and balance cryolite). Results from the operation of this cell are summarized in FIGS. 10 to 12 of the drawings and in Table 2 below. Table 2 compares the operation of the cell of FIGS. 5 and 7 with that of a conventional cell having a metal pad.
  • FIG. 10 compares these embodiments with a drained cell, having a primary cathode slope of 8° in the longitudinal direction of the anode, and a secondary cathode slope of 0° in the transverse direction of the anode (known as 8°/0°), according to the Boxall et al patent referred to above. It is evident from FIG. 11 that thebubble layer resistance decreased as the longitudinal anode angle was increased from 0° to 8° although there was only a minor benefit gain from increasing the anode angle above about 4°. Venting of all bubbles across the anode width into the spaces between anodes yielded a reduced bubble layer resistance beneath the anode and this led to a reduced cell voltage. The effect of bubble path length on resistivity ratio is illustrated in FIG. 12.
  • FIGS. 13 and 14 of the drawings A protrusion/abutment arrangement for achieving a desired electrolyte bath flow and controlled bubble release in a different manner to that describedabove is shown schematically in FIGS. 13 and 14 of the drawings in which angularly positioned cathode protrusions 37, 38, 39 and 40 extend angularly inwardly from the edges of the anode shadow 41, and a further cathode abutment 42 is formed at the outer edge of the anode shadow 41 adjacent the side channel or side wall of the cell.
  • This protrusion arrangement may be particularly advantageous if the anodes to be used are large.
  • the positioning of the angular protrusions 37 to 40 causes channels 43 and 44 to be profiled within the anode 1, as shown in FIG. 14, to give more concentrated gas venting within specific regions of the anode, which in turn reduces the bubble path length of the bubbles under most of the anode.
  • the position and size of each protrusion to be used will depend upon the dimensions of the cell and its operating characteristics. Electrical modelling can be used to assist in the design of the cell in this regard.
  • the height and width of the protrusions would typically be similar to those as shown and described in relation to FIG. 1of the drawings. This type of arrangement may be attractive where dimensionally stable anodes are being used (inert anodes) or continuous pre-baked blocks, since the anode profile may be more easily maintained throughout the operation of the cell by the use of this type of protrusion.
  • the outermost edges of the anodes would be suitably shaped prior to installation and the cathode protrusions would not be required for profiling, although some shaping of the floor and side wall of the cell may be necessary for metal storage to allow a reduced ACD, or to promote proper electrolyte flow, and to provide the necessary cooperative shapes in the anode and cathode for a good parallel geometric fit.
  • the cathode protrusion may take the form of a shaped floor and wall portion of the cell rather than a distinct abutment as shown in FIG. 8 of the drawings.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Electrolytic Production Of Metals (AREA)
  • Battery Electrode And Active Subsutance (AREA)
US07/969,850 1990-08-20 1991-08-19 Aluminium smelting cell Expired - Lifetime US5330631A (en)

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AUPK184390 1990-08-20
AUPK1843 1990-08-20
PCT/AU1991/000372 WO1992003597A1 (en) 1990-08-20 1991-08-19 Improved aluminium smelting cell

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EP (2) EP0544737B1 (de)
BR (2) BR9106775A (de)
CA (2) CA2088482C (de)
DE (2) DE69120081D1 (de)
IS (2) IS3747A7 (de)
NO (1) NO307525B1 (de)
NZ (2) NZ239472A (de)
WO (2) WO1992003598A1 (de)

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5683559A (en) 1994-09-08 1997-11-04 Moltech Invent S.A. Cell for aluminium electrowinning employing a cathode cell bottom made of carbon blocks which have parallel channels therein
US6436273B1 (en) * 1998-02-11 2002-08-20 Moltech Invent S.A. Drained cathode aluminium electrowinning cell with alumina distribution
US6511590B1 (en) * 2000-10-10 2003-01-28 Alcoa Inc. Alumina distribution in electrolysis cells including inert anodes using bubble-driven bath circulation
US6558526B2 (en) * 2000-02-24 2003-05-06 Alcoa Inc. Method of converting Hall-Heroult cells to inert anode cells for aluminum production
US6682643B2 (en) * 1999-04-16 2004-01-27 Moltech Invent S.A. Aluminium electrowinning cells having a V-shaped cathode bottom and method of producing aluminium
US20040163967A1 (en) * 2003-02-20 2004-08-26 Lacamera Alfred F. Inert anode designs for reduced operating voltage of aluminum production cells
US20050199488A1 (en) * 2004-03-11 2005-09-15 Barclay Ron D. Closed end slotted carbon anodes for aluminum electrolysis cells
US20070125643A1 (en) * 2004-03-11 2007-06-07 Alcoa Inc. Closed end slotted carbon anodes for aluminum electrolysis cells
WO2012025498A1 (de) * 2010-08-23 2012-03-01 Sgl Carbon Se Kathode, vorrichtung zur aluminiumgewinnung und verwendung der kathode bei der aluminiumgewinnung
WO2012159839A3 (de) * 2011-05-23 2013-03-28 Sgl Carbon Se Elektrolysezelle und kathode mit unregelmässiger oberflächenprofilierung
WO2013170299A1 (en) * 2012-05-16 2013-11-21 Lynas Services Pty Ltd Electrolytic cell for production of rare earth metals
WO2013170310A1 (en) * 2012-05-16 2013-11-21 Lynas Services Pty Ltd Drained cathode electrolysis cell for production of rare earth metals

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EP0996773B1 (de) * 1997-07-08 2007-06-20 MOLTECH Invent S.A. Zell für aluminium-herstellung mit drainierfähige kathode
CN100478500C (zh) * 2007-03-02 2009-04-15 冯乃祥 一种异形阴极碳块结构铝电解槽
DE102010041083A1 (de) * 2010-09-20 2012-03-22 Sgl Carbon Se Elektrolysezelle zur Gewinnung von Aluminium
DE102011004010A1 (de) * 2011-02-11 2012-08-16 Sgl Carbon Se Kathodenanordnung mit einem oberflächenprofilierten Kathodenblock mit Nut variabler Tiefe
DE102011004011A1 (de) * 2011-02-11 2012-08-16 Sgl Carbon Se Kathodenanordnung mit einem oberflächenprofilierten Kathodenblock mit einer mit Graphitfolie ausgekleideten Nut variabler Tiefe
US9340887B2 (en) * 2013-03-13 2016-05-17 Alcoa, Inc. Systems and methods of protecting electrolysis cells

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Cited By (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5683559A (en) 1994-09-08 1997-11-04 Moltech Invent S.A. Cell for aluminium electrowinning employing a cathode cell bottom made of carbon blocks which have parallel channels therein
US5888360A (en) 1994-09-08 1999-03-30 Moltech Invent S.A. Cell for aluminium electrowinning
US6436273B1 (en) * 1998-02-11 2002-08-20 Moltech Invent S.A. Drained cathode aluminium electrowinning cell with alumina distribution
US6682643B2 (en) * 1999-04-16 2004-01-27 Moltech Invent S.A. Aluminium electrowinning cells having a V-shaped cathode bottom and method of producing aluminium
US6558526B2 (en) * 2000-02-24 2003-05-06 Alcoa Inc. Method of converting Hall-Heroult cells to inert anode cells for aluminum production
US6511590B1 (en) * 2000-10-10 2003-01-28 Alcoa Inc. Alumina distribution in electrolysis cells including inert anodes using bubble-driven bath circulation
US20040163967A1 (en) * 2003-02-20 2004-08-26 Lacamera Alfred F. Inert anode designs for reduced operating voltage of aluminum production cells
US7820027B2 (en) 2004-03-11 2010-10-26 Alcoa, Inc. Method for electrolytically producing aluminum using closed end slotted carbon anodes
US7179353B2 (en) 2004-03-11 2007-02-20 Alcoa Inc. Closed end slotted carbon anodes for aluminum electrolysis cells
US20070125660A1 (en) * 2004-03-11 2007-06-07 Alcoa Inc. Closed end slotted carbon anodes for aluminum electrolysis cells
US20070125643A1 (en) * 2004-03-11 2007-06-07 Alcoa Inc. Closed end slotted carbon anodes for aluminum electrolysis cells
US7799189B2 (en) 2004-03-11 2010-09-21 Alcoa Inc. Closed end slotted carbon anodes for aluminum electrolysis cells
US20050199488A1 (en) * 2004-03-11 2005-09-15 Barclay Ron D. Closed end slotted carbon anodes for aluminum electrolysis cells
JP2013536321A (ja) * 2010-08-23 2013-09-19 エスゲーエル カーボン ソシエタス ヨーロピア アルミニウム生産のためのカソード、装置およびアルミニウム生産におけるカソードの使用
CN103140609A (zh) * 2010-08-23 2013-06-05 西格里碳素欧洲公司 用于生产铝的阴极、装置和所述阴极在生产铝中的用途
WO2012025498A1 (de) * 2010-08-23 2012-03-01 Sgl Carbon Se Kathode, vorrichtung zur aluminiumgewinnung und verwendung der kathode bei der aluminiumgewinnung
WO2012159839A3 (de) * 2011-05-23 2013-03-28 Sgl Carbon Se Elektrolysezelle und kathode mit unregelmässiger oberflächenprofilierung
CN103635610A (zh) * 2011-05-23 2014-03-12 西格里碳素欧洲公司 电解槽以及具有不规则表面造型的阴极
JP2014517876A (ja) * 2011-05-23 2014-07-24 エスゲーエル カーボン ソシエタス ヨーロピア 電解セルおよび不規則な表面プロファイリングを有するカソード
WO2013170299A1 (en) * 2012-05-16 2013-11-21 Lynas Services Pty Ltd Electrolytic cell for production of rare earth metals
WO2013170310A1 (en) * 2012-05-16 2013-11-21 Lynas Services Pty Ltd Drained cathode electrolysis cell for production of rare earth metals
AU2013204396B2 (en) * 2012-05-16 2015-01-29 Lynas Services Pty Ltd Electrolytic cell for production of rare earth metals
CN104520476A (zh) * 2012-05-16 2015-04-15 莱纳服务有限公司 用于稀土金属的生产的电解池
RU2620319C2 (ru) * 2012-05-16 2017-05-24 Лайнас Сервисез Пти Лтд Электролитическая ячейка для производства редкоземельных металлов
CN104520476B (zh) * 2012-05-16 2017-12-12 莱纳服务有限公司 用于稀土金属的生产的电解池

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WO1992003597A1 (en) 1992-03-05
IS3747A7 (is) 1992-02-21
BR9106774A (pt) 1993-08-24
EP0550456A1 (de) 1993-07-14
CA2088482A1 (en) 1992-02-21
DE69120081D1 (de) 1996-07-11
WO1992003598A1 (en) 1992-03-05
BR9106775A (pt) 1993-08-24
CA2088483C (en) 2000-10-10
EP0550456B1 (de) 1995-11-08
EP0544737B1 (de) 1996-06-05
NZ239473A (en) 1993-09-27
EP0550456A4 (en) 1993-10-27
NO307525B1 (no) 2000-04-17
CA2088482C (en) 2000-12-26
IS3746A7 (is) 1992-02-21
NO930563D0 (no) 1993-02-17
NO930563L (no) 1993-02-17
EP0544737A1 (de) 1993-06-09
EP0544737A4 (en) 1993-10-27
NZ239472A (en) 1993-06-25
DE69114511D1 (de) 1995-12-14

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